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United States · US · US:42291-713_2b47ad1c-e1cb-7b8b-e063-6394a90aee3c
ROPINIROLE HYDROCHLORIDE
Orange BookUNIISPLATC N04BC04
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerAvKARE
CountryUS (United States)
ATC codeN04BC04
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc11422917133030 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (42291-713-30)
Annotations
UNII (FDA Substance ID)
D7ZD41RZI9
ROPINIROLE HYDROCHLORIDE
RxCUI 236553
Orange Book
A090869
ABABABABAB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "D7ZD41RZI9",
"rxcui": "236553",
"inchikey": "XDXHAEQXIBQUEZ-UHFFFAOYSA-N",
"display_name": "ROPINIROLE HYDROCHLORIDE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"c89f68e5-d2ad-4aad-a63c-c32eff5e82c9": {
"match": "brand_token",
"title": "ROPINIROLE TABLET, FILM COATED [BRYANT RANCH PREPACK]",
"spl_version": "101",
"published_date": "2026-06-01"
}
},
"productid": "42291-713_2b47ad1c-e1cb-7b8b-e063-6394a90aee3c",
"productndc": "42291-713",
"dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE",
"orange_book": {
"appl_no": "090869",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "EQ 2MG BASE",
"product_no": "001",
"approval_date": "May 17, 2012"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "EQ 4MG BASE",
"product_no": "002",
"approval_date": "May 17, 2012"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "EQ 6MG BASE",
"product_no": "003",
"approval_date": "May 17, 2012"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "EQ 8MG BASE",
"product_no": "004",
"approval_date": "May 17, 2012"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "EQ 12MG BASE",
"product_no": "005",
"approval_date": "May 17, 2012"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "ROPINIROLE HYDROCHLORIDE",
"proprietary_name": "ROPINIROLE HYDROCHLORIDE",
"active_ingred_unit": "mg/1",
"application_number": "ANDA090869",
"marketing_category": "ANDA",
"nonproprietary_name": "ropinirole hydrochloride",
"start_marketing_date": "20130913",
"active_numerator_strength": "2"
}Related drugs
Other records sharing ATC code N04BC04.
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